BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PURELL HAND SANITIZER

    MDR report key: 23862463 · Received December 22, 2025

    Report

    Report Number
    MW5180847
    Event Type
    Injury
    Date Received
    December 22, 2025
    Date of Event
    December 5, 2025
    Report Date
    December 15, 2025
    Manufacturer
    MEDLINE INDUSTRIES, LP - NORTHFIELD
    Product Code
    LRJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    DESCRIPTION OF REPORTED EVENT: A PERITONEAL DIALYSIS (PD) PATIENT CONTACTED (B)(6) CUSTOMER SERVICE TO REPORT THAT WHEN SHE USES THE PURELL HAND SANITIZER ENDS UP GETTING A RASH AND BREAKS OUT THE HANDS WHEN USED. PATIENT WANTED CUSTOMER SERVICE TO KNOW SINCE UNABLE TO USE. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2281322 PURELL HAND SANITIZER DISINFECTANT, MEDICAL DEVICES LRJ MEDLINE INDUSTRIES, LP - NORTHFIELD

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown